Hydrogen production by photoreforming of biofuels using Au, Pd and Au-Pd/TiO2 photocatalysts

被引:103
|
作者
Bowker, M. [1 ,2 ]
Morton, C. [1 ]
Kennedy, J. [1 ]
Bahruji, H. [1 ]
Greves, J. [1 ]
Jones, W. [1 ,2 ]
Davies, P. R. [1 ]
Brookes, C. [1 ,2 ]
Wells, P. P. [2 ]
Dimitratos, N. [2 ]
机构
[1] Cardiff Univ, Sch Chem, Cardiff Catalysis Inst, Cardiff CF10 3AT, S Glam, Wales
[2] Rutherford Appleton Lab, Ctr Catalyt Sci, Harwell OX11 0F, Oxon, England
基金
英国工程与自然科学研究理事会;
关键词
Alcohols; Au catalysts; Pd catalysts; Biofuels; Photoreforming; Hydrogen production; Solar fuels; SOLVENT-FREE OXIDATION; FORMIC-ACID; METHANOL; OXYGEN; CATALYSTS; WATER; DECOMPOSITION; ADSORPTION; GLYCEROL; SURFACE;
D O I
10.1016/j.jcat.2013.04.005
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We have prepared a variety of Au, Pd and Au-Pd catalysts loaded onto P25 titania to determine how effective these materials are for the anaerobic, ambient temperature reforming of alcohols with water to produce hydrogen, and to examine the effect of the preparation method on their performance. Catalysts produced by both incipient wetness (IW) methods and by colloidal methods are successful materials for producing hydrogen, with the IW catalysts proving to be the best for the same metal loading. It is shown that, although gold catalysts generally have lower hydrogen yield than for Pd, alloying Au with Pd gives more active materials than either alone at the same weight loading, due to a synergistic effect. The catalysts are active for reforming a range of alcohols, generally producing CO2, H-2 and an alkane. However, it is essential for good activity to have an H at the alpha-position to the oxygenate function, and so, carboxylic acids and ketones do not work. These catalysts generally show a maximum in activity at low loadings of metal (similar to 0.5 wt%) due to a requirement for maximising the active interface between the metal nanoparticles and the photo-active titania. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:10 / 15
页数:6
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